Canonical Allele Identifier: PA2827998160
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41512
ClinVar RCV Id: RCV000034397 RCV000120030 RCV000115118 RCV000515182 RCV001083312 RCV001153053 RCV003650356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2287Ser
CA012759
NM_001354901.2:c.6859C>T